Indications and uses
heatburn sour stomach acid indigestion
Rapidol Sodium Bicarbonate - Pharmadel LLC
- Manufacturer
- Pharmadel LLC
- Effective date
- 2026-03-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 01:51:45
Label at a glance#
ProductRapidol Sodium Bicarbonate
Active ingredientSODIUM BICARBONATE
Label structure8 sections
Dosage and administration
do not take more than your “ maximum daily dosage for your age group ” in a 24-hour period. See Warnings. take a ½ teaspoon in a 4 fl. oz. (½ a glass) of water every 2 hours up to the maximum daily dosage or as directed by a doctor dissolve completely in water before drinking age maximum daily dosage adults 60 years of age and over ½ teaspoon, 3 times a day adults under 60 and children 12 years of age and over ½ t...
Contacts and useful links#
Websitewww.pharmadel.com
www.pharmadel.com
www.pharmadel.comLabel contents#
Full prescribing information#
Active Ingredient & Purposes
OTC - PURPOSE SECTION
| Active ingredient (in each ½ teaspoon) | Purpose |
| Sodium bicarbonate 2,616 mg......................................................................................................... | Antacid |
Uses For the relief of an upset stomach associated with these symptoms
- heatburn
- sour stomach
- acid indigestion
Warnings
Stomach Waring: To avoid serious injury, do not take powder until it is completely dissolved. It is very important not to take this product when overly full from food or drink. Consult a doctor if severe stomach pain occurs after taking this product.
Do not use
- the maximum daily dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor
- this product except under advice and supervision of a physician if you are allergic to milk or milk products
When using this product
- may cause constipation
- may have laxative effect
Ask a doctor or pharmacist before use if you are
- presently taking a prescription drug. Antacids may interact with certain prescription drugs.
Ask a doctor before use if you have
- a sodium-restricted diet
If pregnant or breast-feeding,
ask a health professional before use.
KEEP OUT OF REACH OF CHILDREN.
In case of an accidental overdose, seek professional assistance or contact a Poison Control center right away.
Directions
- do not take more than your “ maximum daily dosage for your age group” in a 24-hour period. See Warnings.
- take a ½ teaspoon in a 4 fl. oz. (½ a glass) of water every 2 hours up to the maximum daily dosage or as directed by a doctor
- dissolve completely in water before drinking
| age | maximum daily dosage |
| adults 60 years of age and over | ½ teaspoon, 3 times a day |
| adults under 60 and children 12 years of age and over | ½ teaspoon, 6 times a day |
| children under 12 years of age | do not use |
Other information
- each ½ teaspoonful contains: sodium 716 mg
- store in cool dry place below 77ºF
- do not use if seal under cap is torn, broken or missing
INACTIVE INGREDIENT SECTION
None
Questions & comments?
Prinicpal Display Panel
55758-327-04
4 Oz
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| BICARBONATE ION Pharmacologic Class Indexing | 1 | Indexing - Pharmacologic Class | 20220121 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55758-319-04 | Rapidol Sodium Bicarbonate | 113 g in 1 BOTTLE | POWDER | 113 | 4 |
Products#
Every source-derived product name is available through these pages.
- Rapidol Sodium Bicarbonate
- Sodium Bicarbonate
- BICARBONATE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55758-319 | 55758-319-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM BICARBONATE | 8MDF5V39QO | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 3 | 2025-12-04 | monthly-update | 2026-06-03 17:45:23 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Rapidol Sodium Bicarbonate | SODIUM BICARBONATE | Pharmadel LLC | b4c9a653-6f51-7c98-e053-2995a90ada37 | 2026-03-26 | Warnings | 55758-319-04 55758-319 55758031904 4df255cd-f223-1b0c-e063-6394a90ad6f7 b4c9a653-6f51-7c98-e053-2995a90ada37 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.